Involvement of ASK1 in Ca2+-induced p38 MAP kinase activation

被引:153
作者
Takeda, K
Matsuzawa, A
Nishitoh, H
Tobiume, K
Kishida, S
Ninomiya-Tsuji, J
Matsumoto, K
Ichijo, H
机构
[1] Univ Tokyo, Grad Sch Pharmaceut Sci, Lab Cell Signaling, Bunkyo Ku, Tokyo 1130033, Japan
[2] Japan Sci & Technol Corp, CREST, Bunkyo Ku, Tokyo 1130033, Japan
[3] Tokyo Med & Dent Univ, Grad Sch, Lab Cell Signaling, Tokyo, Japan
[4] Nippon Med Coll, Inst Gerontol, Dept Mol Oncol, Kawasaki, Kanagawa, Japan
[5] Nagoya Univ, Grad Sch Sci, Dept Mol Biol, Nagoya, Aichi, Japan
[6] Japan Soc & Technol Corp, CREST, Nagoya, Aichi, Japan
关键词
D O I
10.1038/sj.embor.7400072
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The mammalian mitogen-activated protein (MAP) kinase kinase kinase apoptosis signal-regulating kinase 1 (ASK1) is a pivotal component in cytokine- and stress-induced apoptosis. It also regulates cell differentiation and survival through p38 MAP kinase activation. Here we show that Ca2+ signalling regulates the ASK1-p38 MAP kinase cascade. Ca2+ influx evoked by membrane depolarization in primary neurons and synaptosomes induced activation of p38, which was impaired in those derived from ASK1-deficient mice. Ca2+/calmodulin-dependent protein kinase type II (CaMKII) activated ASK1 by phosphorylation. Moreover, p38 activation induced by the expression of constitutively active CaMKII required endogenous ASK1. Thus, ASK1 is a critical intermediate of Ca2+ signalling between CaMKII and p38 MAP kinase.
引用
收藏
页码:161 / 166
页数:6
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